WO2002020845A3 - Ultra yield amplification reaction - Google Patents
Ultra yield amplification reaction Download PDFInfo
- Publication number
- WO2002020845A3 WO2002020845A3 PCT/US2001/028028 US0128028W WO0220845A3 WO 2002020845 A3 WO2002020845 A3 WO 2002020845A3 US 0128028 W US0128028 W US 0128028W WO 0220845 A3 WO0220845 A3 WO 0220845A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- nucleic acid
- target nucleic
- amplification reaction
- reaction
- primer
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6844—Nucleic acid amplification reactions
- C12Q1/686—Polymerase chain reaction [PCR]
Abstract
The sensitivity, and therefore specificity, of the polymerase chain reaction is compromised by primer-dimer formation early in the amplification process. Described herein is a simple and novel technique to avoid the formation of primer-dimers. A target nucleic acid is first amplified in a 'pre-amplification' reaction, wherein an extremely low concentration of primers bind to the target nucleic acid and not to each other. This allows for the efficient use of the DNA polymerase, deoxynucleoside triphosphates and other reaction components, to extend and amplify the target nucleic acid.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US23126300P | 2000-09-08 | 2000-09-08 | |
US60/231,263 | 2000-09-08 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2002020845A2 WO2002020845A2 (en) | 2002-03-14 |
WO2002020845A3 true WO2002020845A3 (en) | 2003-03-13 |
Family
ID=22868459
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2001/028028 WO2002020845A2 (en) | 2000-09-08 | 2001-09-06 | Ultra yield amplification reaction |
Country Status (2)
Country | Link |
---|---|
US (1) | US20020031777A1 (en) |
WO (1) | WO2002020845A2 (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7695941B2 (en) * | 2005-06-16 | 2010-04-13 | The United States Of America As Represented By The Secretary Of The Navy | Multiplexed polymerase chain reaction for genetic sequence analysis |
EP1666150B1 (en) | 2004-11-20 | 2015-01-07 | Roche Diagnostics GmbH | Nucleic acid preparation |
EP1658898A1 (en) * | 2004-11-20 | 2006-05-24 | Roche Diagnostics GmbH | Nucleic acid preparation |
DE102006003990A1 (en) * | 2006-01-23 | 2007-08-02 | Gebr. Schmid Gmbh & Co. | Method and device for processing or processing silicon material |
US7833716B2 (en) | 2006-06-06 | 2010-11-16 | Gen-Probe Incorporated | Tagged oligonucleotides and their use in nucleic acid amplification methods |
EP2121956B1 (en) | 2006-12-21 | 2016-08-17 | Gen-Probe Incorporated | Methods and compositions for nucleic acid amplification |
US7888858B2 (en) | 2007-08-21 | 2011-02-15 | Global Oled Technology Llc | Light emitting diode device incorporating a white light emitting layer in combination with a plurality of optical microcavities |
US9169512B2 (en) | 2009-07-01 | 2015-10-27 | Gen-Probe Incorporated | Methods and compositions for nucleic acid amplification |
KR101287431B1 (en) * | 2010-05-07 | 2013-07-19 | (주)진매트릭스 | Primer composition for amplifying genetic region having various genetic variations in target genes, method for amplifying the target genes using the same, PCR amplification kit comprising the same and method for analyzing the genotype of the target genes |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0469610A1 (en) * | 1990-08-02 | 1992-02-05 | SHIONOGI SEIYAKU KABUSHIKI KAISHA trading under the name of SHIONOGI & CO. LTD. | Improved two-step PCR method |
EP0866071A2 (en) * | 1997-03-20 | 1998-09-23 | F. Hoffmann-La Roche Ag | Modified primers |
-
2001
- 2001-09-06 US US09/948,336 patent/US20020031777A1/en not_active Abandoned
- 2001-09-06 WO PCT/US2001/028028 patent/WO2002020845A2/en active Application Filing
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0469610A1 (en) * | 1990-08-02 | 1992-02-05 | SHIONOGI SEIYAKU KABUSHIKI KAISHA trading under the name of SHIONOGI & CO. LTD. | Improved two-step PCR method |
EP0866071A2 (en) * | 1997-03-20 | 1998-09-23 | F. Hoffmann-La Roche Ag | Modified primers |
Non-Patent Citations (3)
Title |
---|
BROWNIE JANNINE ET AL: "The elimination of primer-dimer accumulation in PCR", NUCLEIC ACIDS RESEARCH, OXFORD UNIVERSITY PRESS, SURREY, GB, vol. 25, no. 16, 1997, pages 3235 - 3241, XP002152588, ISSN: 0305-1048 * |
ERLICH H.A.: "PCR technology, Principles and Applications for DNA Amplification", 1989, STOCKTON PRESS, NEW YORK, US, XP002223319 * |
GIBBS ET AL: "DIAGNOSIS OF NEW MUTATION DISEASES USING THE POLYMERASE CHAIN REACTION", PCR TECHNOLOGY. PRINCIPLES AND APPLICATIONS FOR DNA AMPLIFICATION, NEW YORK, STOCKTON PRESS, US, 1989, pages 171 - 190, XP000886474 * |
Also Published As
Publication number | Publication date |
---|---|
US20020031777A1 (en) | 2002-03-14 |
WO2002020845A2 (en) | 2002-03-14 |
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